The prevalence of an uncommon allelic variant (S2) of the apoprotein AI-CIII-AIV gene cluster was determined in non-insulin-dependent diabetics with or without evidence of coronary heart disease and in controls. Frequencies of the S2 allele were 14% for diabetics with coronary heart disease compared with 2% for non-diabetics with no clinical evidence of occlusive vascular disease. No subject with the S2 allele was detected among a further group of matched diabetics without Clinical features of macro vascular disease. The results suggest that a genetic component contributes to the susceptibility to coronary heart disease in non-insulin-dependent diabetics. Whether the observed deoxyribonucleic acid variant is aetiological for atherosclerosis or in linkage disequilibrium with other atherogenic loci on chromosome 11 remains to be clarified. © 1987, British Medical Journal Publishing Group. All rights reserved.
CITATION STYLE
Trembath, R. C., Thomas, D. J. B., Hendra, T. J., Yudkin, J. S., & Galton, D. I. (1987). Deoxyribonucleic acid polymorphism of the apoprotein AI-CIII-AIV gene cluster and coronary heart disease in non-insulin-dependent diabetes. British Medical Journal (Clinical Research Ed.), 294(6587), 1577–1578. https://doi.org/10.1136/bmj.294.6587.1577
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